BEUDAMED
    610 results · 25ms · Sources: EU EUDAMED, US FDA

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    OVERLANDER PEV 2000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PEV 2000

    FDA Adverse Event
    Malfunction ·WHEELCHAIRS OF KANSAS·Product code ITI·October 16, 2012

    OVERLANDER- PEV2000

    FDA Adverse Event
    Malfunction ·RAYE'S, INC., DBA, WHEELCHAIRS OF KANSAS·Product code ITI·September 6, 2001

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 8, 2014

    Plateau

    FDA UDI
    Respironics, Inc.·00606959020177·Plateau Exhalation Valve (PEV), Single, Reusable

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·October 19, 2016

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·October 19, 2016

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·June 6, 2019

    PEV 2000 - OVERLANDER POWER WHEELCHAIR

    FDA Adverse Event
    Malfunction ·RAYES, INC. DBA WHEELCHAIRS OF KANSAS·Product code ITI·August 28, 2008

    IMPL.DRIVER P EV 4.2 LONG

    FDA Adverse Event
    Malfunction ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code NDP·January 30, 2026

    IMPL.DRIVER P EV 4.8 SHORT

    FDA Adverse Event
    Malfunction ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code NDP·January 6, 2026

    SENZA

    FDA Adverse Event
    Malfunction ·NEVRO CORP.·Product code LGW·April 17, 2023

    ALPHA IV PEV.2,30MM ACTIVE TRANSFER DEVICE

    FDA Adverse Event
    Malfunction ·NOVOSTE CORPORATION·Product code MOU·January 16, 2002

    PEV POR SHL W/SEALABLE SCWHLS SZ63MM

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·April 23, 2002

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·October 12, 2020

    OPTEASE RETRIEVAL FILTER

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·February 21, 2019

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·August 29, 2018

    JRNY II CR FEM OX NP RT SZ 5

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·September 29, 2020

    TRAPEASE PVCF FEM/JUG 55CM CSI

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·June 17, 2020

    PERFECTO2 V WITH SENSOR 9153650799

    FDA Adverse Event
    Malfunction ·Product code CAW·July 15, 2021